United States · FDA National Drug Code directory
carboprost tromethamine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70121-1680_ec46a8fb-b01e-4e93-950a-a3c34203e351
- Product NDC
- 70121-1680
- Form
- INJECTION, SOLUTION
- Composition / generic term
- carboprost tromethamine
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220130
- Source listing expiry
- 20261231
Source-listed ingredients
- CARBOPROST TROMETHAMINE — 250 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (70121-1680-1) / 1 mL in 1 VIAL · 70121-1680-1
- 10 VIAL in 1 CARTON (70121-1680-7) / 1 mL in 1 VIAL · 70121-1680-7
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →